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  • 化合物 NMDA receptor antagonist 4|T60306|TargetMol

化合物 NMDA receptor antagonist 4|T60306|TargetMol

NMDA receptor antagonist 4
询价 25mg 起订
50mg 起订
100mg 起订
上海 更新日期:2025-11-17

TargetMol中国(陶术生物)

VIP2年
联系人:邵小姐
手机:15002134094 拨打
邮箱:marketing@targetmol.cn

产品详情:

中文名称:
化合物 NMDA receptor antagonist 4
英文名称:
NMDA receptor antagonist 4
CAS号:
1607589-56-9
品牌:
TargetMol
产地:
美国
保存条件:
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
产品类别:
抑制剂
货号:
T60306

Product Introduction

Bioactivity

名称NMDA receptor antagonist 4
描述NMDA receptor antagonist 4 (IIc) is an uncompetitive, voltage-dependent, orally active NMDAR blocker, with an IC 50 of 1.93 μM. NMDA receptor antagonist 4 shows a positive predicted blood-brain-barrier (BBB) permeability, and can be used in Alzheimer's disease research[1].
体外活性NMDA receptor antagonist 4 (IIc) exhibits competitive interaction with endogenous blocker Mg 2+, and exhibits dependence on membrane potential in the NMDAR channel [1]. NMDA receptor antagonist 4 shows high metabolic stability in human and mice liver microsomes, and shows hERG safety, without obvious cytotoxicity [1]. Cell Cytotoxicity Assay [1] Cell Line: Neuro2A cells Concentration: 1, 10, and 100 μM Incubation Time: 24 h Result: Did not show cytotoxic at the highest concentration tested (100 μM).
体内活性NMDA receptor antagonist 4 (IIc) (0-10 μM) lowers the motor deficits, and protects against Aβ toxicity-related neuronal dysfunction [1]. NMDA receptor antagonist 4 (5 mg/kg/day; p.o.; 4 weeks) improves cell survival and synaptic function in AD through increasing the activity of cell-survival signaling pathways (Fyn-GluN2B-CREB signaling) and preventing internalization of synaptic NMDARs [1]. Animal Model: C. elegans (N2 wild-type, CL2006, CL2122, CL2355) [1] Dosage: 0, 0.1, 0.5, 1.5, and 10 μM Administration: Result: Reduced defective locomotion in CL2006 nematodes. Significantly reversed the chemotaxis behavior of CL2355 nematodes disrupted by Aβ expression. Animal Model: Six months old female 5XFAD mice [1] Dosage: 5 mg/kg/day Administration: Oral administration, 4 weeks Result: Enhanced working memory function. Rescued the expression of GluN2A and postsynaptic density protein (PSD) 95. Increased Fyn phosphorylated levels and correspondingly elevated GluN2B phosphorylation at Tyr1472. Significantly increased p-CREB protein levels in the nucleus. Reverted calbindin D-28K protein levels.
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
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NMDA receptor antagonist 4|TargetMol

公司简介

TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。

成立日期 (13年)
注册资本 589.8595万人民币
员工人数 100-500人
年营业额 ¥ 1亿以上
经营模式 贸易,工厂,试剂,定制,服务
主营行业 中间体,天然产物,生物化工,化学试剂,生物技术服务

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